A New β0-Thalassemia Mutation (codon 102, AAC>ATCAC) in Coexistence with a HeterozygousP4.2 NipponGene-Reference-Cited by-同舟云学术

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A New β0-Thalassemia Mutation (codon 102, AAC>ATCAC) in Coexistence with a HeterozygousP4.2 NipponGene

Published:2013-04-22 Issue:3 Volume:37 Page:227-240
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Adhiyanto Chris,Yamashiro Yasuhiro,Hattori Yukio,Nitta Takenori,Hino Minako,Matar Maryam,Takagi Fumiya,Kimoto Masafumi

Publisher

Informa UK Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2013.777847

Reference32 articles.

1. Bridges KR, Pearson HA, Eds. Thalassemia. Anemia and Other Red Cell Disorders, 1st ed. New York: McGraw Hill. 2008:277–301.

2. Dominantly Inherited β-Thalassemia

3. RED BLOOD CELL INDEXES IN PATIENTS WITH HEREDITARY SPHEROCYTOSIS AND β-THALASSEMIA COMBINATION

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1. Novel mechanism of hereditary pyropoikilocytosis phenotype due to co‐inheritance of β globin and α spectrin mutations;American Journal of Hematology;2021-02-25

2. A Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the SPTB Gene Misdiagnosed as β-Thalassemia Intermedia Due to a KLF1 Gene Mutation;Hemoglobin;2019-03-04

3. A Coincidental Discovery of a New Stable Variant (Hb Hachioji orHBB: c.187C>T) in a Patient with Chronic Hemolytic Anemia of Unexplained Origin;Hemoglobin;2018-01-02

4. Haemoglobin variants may cause significant differences in haemoglobin A1c as measured by high-performance liquid chromatography and enzymatic methods in diabetic patients: a cross-sectional study;Annals of Clinical Biochemistry: International Journal of Laboratory Medicine;2016-08-05

5. A Rare Case of Variant Hemoglobin (Hb Yahata) Suspected Based on Inconsistent Plasma Glucose and HbA1c Levels;Internal Medicine;2015

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